A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169482



Internal ID21313965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:93953388..93968763hg38UCSC Ensembl
Outerchr10:93944122..93969447hg38UCSC Ensembl
Innerchr10:95713145..95728520hg19UCSC Ensembl
Outerchr10:95703879..95729204hg19UCSC Ensembl
Innerchr10:95703135..95718510hg18UCSC Ensembl
Outerchr10:95693869..95719194hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3825326
hg1925326
hg1825326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14251166
SamplesPML_3
Known GenesPIPSL
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169482
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer